Indications and uses
For the temporary relief of minor aches and pains of muscles and joints associated with ● arthritis ● simple backache ● strains ● bruises ● sprains
Arthritis Wonder
- Manufacturer
- G2 Products LLC
- Effective date
- 2020-03-27
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:05:03
Label at a glance#
ProductArthritis Wonder
Active ingredientMENTHOL
Label structure7 sections
Dosage and administration
• Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily • Children under 2 years of age: consult a doctor
Label contents#
Full prescribing information#
Active ingredient
Menthol 1.25%
Purpose
External analgesic
Uses
For the temporary relief of minor aches and pains of muscles and joints associated with ● arthritis ● simple backache ● strains ● bruises ● sprains
Warnings
For external use only.
Flammable: Keep away from fire or flame.
When using this product
• avoid contact with the eyes • do not bandage tightly
Do not use
● on wounds or damaged skin with a heating pad
Stop use and ask a doctor if
• condition worsens • symptoms persist for more than 7 days • symptoms clear up and occur again within a few days
Keep out of the reach of children
If swallowed, get medical help or contact a Poison Control Center right away
Directions
• Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily • Children under 2 years of age: consult a doctor
Inactive ingredients:
Alcohol, Caprylic/Capric Triglyceride, Caprylyl Glycol, Cetearyl Alcohol, Cetyl Alcohol, Dimethicone, Ethoxydiglycol, Ethylhexylglycerin, Glyceryl Oleate, Glyceryl Stearate, Hexylene Glycol, Lecithin, Mentha Piperita (Peppermint) Oil, Phenoxyethanol, Potassium Olivoyl Hydrolyzed Oat Protein, Propanediol, Pullulan, Sclerotium Gum, Sodium Phytate, Water, Wogonin, Xanthan Gum.
Principal Display Panel
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71893-101-20 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-39c0-a426-e053-dadaa90af4c2 | Arthritis Wonder |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71893-101-20 | Arthritis Wonder | 85 g in 1 APPLICATOR | CREAM | 85 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Arthritis Wonder
- Menthol
- DIMETHICONE
- DIETHYLENE GLYCOL MONOETHYL ETHER
- LECITHIN, SOYBEAN
- PHENOXYETHANOL
- GLYCERYL OLEATE
- HEXYLENE GLYCOL
- PEPPERMINT OIL
- PEPPERMINT
- PROPANEDIOL
- PULLULAN
- ETHYLHEXYLGLYCERIN
- WATER
- WOGONIN
- XANTHAN GUM
- ALCOHOL
- MEDIUM-CHAIN TRIGLYCERIDES
- CAPRYLYL GLYCOL
- CETOSTEARYL ALCOHOL
- CETYL ALCOHOL
- GLYCERYL MONOSTEARATE
- CLAVICEPS PURPUREA SCLEROTIUM
- HEXASODIUM PHYTATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71893-101 | 71893-101-20 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| a1cf3a6c-8a94-7a2a-e053-2995a90ae54d | a1cf3a61-b0c6-318d-e053-2995a90a3635 | 2020-03-27 | Warnings | a1cf3a6c-8a94-7a2a-e053-2995a90ae54d a1cf3a61-b0c6-318d-e053-2995a90a3635 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.